Arctic Cat Recalls Snowmobiles Due to Fire Hazard
Reported: February 23, 2010 Initiated: February 23, 2010 #10721
Product Description
The recall involves all Model Year 2010 Arctic Cat 500 Sno Pro models. The model name and number are displayed on the side of the seat and on the engine cowling.
Reason for Recall
Fuel can leak from the fuel pump at the fuel tank mounting screws, posing a fire hazard to consumers.
Remedy
Consumers should stop using these snowmobiles immediately and contact their local Arctic Cat snowmobile dealer to schedule a free repair. Registered owners have been directly notified about this recall by mail.
Details
- Recalling Firm
- Arctic Cat Inc. of Thief River Falls, Minn.
- Units Affected
- About 1,300
Frequently Asked Questions
What product was recalled? ▼
The recall involves all Model Year 2010 Arctic Cat 500 Sno Pro models. The model name and number are displayed on the side of the seat and on the engine cowling.. Recalled by Arctic Cat Inc. of Thief River Falls, Minn.. Units affected: About 1,300.
Why was this product recalled? ▼
Fuel can leak from the fuel pump at the fuel tank mounting screws, posing a fire hazard to consumers.
What should consumers do? ▼
Consumers should stop using these snowmobiles immediately and contact their local Arctic Cat snowmobile dealer to schedule a free repair. Registered owners have been directly notified about this recall by mail.
Which agency issued this recall? ▼
This recall was issued by the CPSC on February 23, 2010. Severity: Moderate. Recall number: 10721.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11